A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997234



Internal ID20564274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11813382..11817846hg38UCSC Ensembl
chr12:11966316..11970780hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg384465
hg194465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462870
Supporting Variants
Samples
Known GenesETV6, RNU6-19P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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